NH, D., JA, M., & JK, B. (2022). Solvent accessibility of E1α and E1β residues with known missense mutations causing pyruvate dehydrogenase complex (PDC) deficiency: Impact on PDC-E1 structure and function. Journal of inherited metabolic disease, 45(3), 557. https://doi.org/10.1002/jimd.12477
Chicago Style (17th ed.) CitationNH, Ducich, Mears JA, and Bedoyan JK. "Solvent Accessibility of E1α and E1β Residues with Known Missense Mutations Causing Pyruvate Dehydrogenase Complex (PDC) Deficiency: Impact on PDC-E1 Structure and Function." Journal of Inherited Metabolic Disease 45, no. 3 (2022): 557. https://doi.org/10.1002/jimd.12477.
MLA (9th ed.) CitationNH, Ducich, et al. "Solvent Accessibility of E1α and E1β Residues with Known Missense Mutations Causing Pyruvate Dehydrogenase Complex (PDC) Deficiency: Impact on PDC-E1 Structure and Function." Journal of Inherited Metabolic Disease, vol. 45, no. 3, 2022, p. 557, https://doi.org/10.1002/jimd.12477.